Form 483

MP Biomedicals Diagnostics Division Form 483, 2017-12-13

FDA issued a Form 483 to MP Biomedicals Diagnostics Division on 2017-12-13 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

MP Biomedicals Diagnostics Division · Solon, United States · Issued December 13, 2017

Overview

  • 12 public-safe observations are available for this inspection.
  • 6 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

13 Dec 2017
21 CFR 820.184

DHR content

Cited by Benjamin J Dastoli

13 Dec 2017
21 CFR 820.184

DHR content

Cited by Benjamin J Dastoli

13 Dec 2017
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Benjamin J Dastoli

13 Dec 2017
21 CFR 820.50(a)

Evaluation of suppliers, contractors, etc., requirements

Cited by Benjamin J Dastoli

13 Dec 2017
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Benjamin J Dastoli

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.75(b)Cited across public-safe Form 483 observations2x
21 CFR 820.86Cited across public-safe Form 483 observations2x
21 CFR 820.90(b)(2)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 12 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere